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NONLINEAR NANOPTICS. M. BERTOLOTTI Università di Roma “La Sapienza” Dipartimento SBAI. Erice 2012. Index. Introduction Linear and Nonlinear Systems Nonlinear Susceptibility Nonlinear Optical Interactions Nonlinearities in Metals Composite Materials
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NONLINEAR NANOPTICS M. BERTOLOTTI Università di Roma “La Sapienza” Dipartimento SBAI Erice 2012
Index Introduction Linear and Nonlinear Systems Nonlinear Susceptibility Nonlinear Optical Interactions Nonlinearities in Metals Composite Materials Erice 2012
Introduction (1) It is now possible to fabricate artificial structures whose chemical compositions and shapes are controlled with a nanometer accuracy. These man-made systems are too small to behave like the bulk parent compounds and too big to behave like atoms or molecules. They may present new properties and because we can tailor some of these for specific purposes, nanostructures have the potential for revolutionary applications in electronics and optics. Furthermore, we know from the basic principle of quantum mechanics that when the size of a system becomes comparable to the characteristic length scale that determines the coherence of the wave functions, quantum size effects occur. The properties then become size and shape dependent.
Introduction (2) Optical properties in particular are very sensitive to quantum confinement. In semiconductors, for example, when a photon is absorbed it creates an electron-hole pair, and the two particles interact strongly by electrostatics. Because the effective masses are small and the dielectric constant large, the exciton (bound state of the electron-hole pair) is large on the atomic scale. Depending on the material, the corresponding Bohr radius a0, which sets the natural length scale for all optical processes, is about 50 Å to 500 Å. One can observe massive changes in optical properties when the dimension of a semiconductor sample, in one or several directions, approaches a0.
Introduction (3) The optical response of a material is the average of the material properties in a volume larger than 3. In ordinary materials the ultimate blocks are atoms or molecules and the optical response is the refractive index n. p dipole moment of the atom, N number of atoms per unit volume. If the material is made by nanostructures with some optical properties, the optical response of the material is an average index nav which can be tailored according to the properties of the nanostructures.
Introduction (4) If the typical dimension of the structure is of the same order of , confinement effects may occur and the structure may behave as a resonant cavity. Some consequences are: - a change of the density of electromagnetic modes, - Electromagnetic field confinement and enhancement, - light velocity may be slowed down or become superluminal, - nonlinear processes may be modified, - suppression or enhancement of spontaneous emission may occur, - thermal radiation distribution may be modified.
Nonlinear Optics Linear and Nonlinear Systems A linear system is defined as one which has a response proportional to an external influence and has a well-known property, i.e. if influences, F1, F2 …., Fn are applied simultaneously, the response produced is the sum of the responses that would be produced if the influences were applied separately. A nonlinear systemis one in which the response is not strictly proportional to the influence and the transfer of energy from one influence to another can occur.
If theinfluences are periodic in time, the response of a nonlinear system can contain frequencies different from those present in the influences. However, the point to emphasize here is that, as well as the generation of new frequencies, nonlinear optics provides the ability to control light with light and so to transfer information directly from one beam to another without the need to resort to electronics. Traditionally, nonlinear optics has been described phenomenologically in terms of the effect of an electric field on the polarization within a material.
MAXWELL EQUATIONS Electromagnetic processes are described by Maxwell’s equations which constitute a set of linear equations. In SI units: where E and B are the electric and magnetic fields. The displacement fields D and H arise from the external charge and conduction current densities and J. In most cases of interest in nonlinear optics, = 0 and J = 0.
Constitutive relations connect the charge and current distributions within the medium and the displacement fields to the electric and magnetic fields. where P is the induced polarization in the medium resulting from the field E, is defined as a dielectric constant and 0 is the permittivity of free space (8.85 × 10-12 F m-1 in MKS units). Optical materials are mostly non magnetic = r 0 = 0.
LINEAR THEORY Usually one assumes a linear response of a dielectric material to an external field where P is the vector representing the electric dipole moment per unit volume induced by the external electric field E, 0 is vacuum permittivity and is a quantity characteristics of the considered material with no dimensions, called electric susceptibility.
In general is a tensor The symmetry properties of the material indicate which ones of the ij coefficients are zero. Alternatively
HOMOGENEOUS MATERIALS not depending on space If
WAVE EQUATION Starting from Maxwell’s Eqs refractive index
DISPERSION Experimentally the refractive index is a function of wavelength (frequency) This phenomenon is called DISPERSION. The polarization in a material medium can be explained considering the electrons tied to the atoms as harmonic oscillators. Nucleus: ~2000 electron mass, i.e., infinite mass
E x DISPERSION (one-dimensional model) Restoring Force Driving Force Damping From the solution: the induced moment is calculated: e-
For N oscillators per volume unit, the polarization is: Calling where is the electric susceptibility.
If the second term is lower than 1 (as it happens in gases): In the expression n comes out to be a complex number.
ABSORPTION The term i is responsible for absorption. The complex index can be written as If we consider a plane wave where
we see that, substituting the complex refractive index, one has which gives The last exponential represents a term of attenuation. The attenuation coefficient may be defined from: By comparison with the previous equation
1 . 0 - 1 0 . 5 ) . u . a ( 0 - 0 . 5 - 3 . 0 - 1 . 5 0 1 . 5 3 . 0 w - w 0 It can be noticed that a small value of leads to an elevated attenuation. Both and are functions of the frequency.
METALS In a metal the electrons are free and they do not oscillate around the atoms. Therefore k = 0 and 0 = 0. In the equation for n2 it is sufficient to put 0 = 0. If << Plasma frequency For Al, Cu, Au, Ag N ~ 1023 cm-3 and P~ 2.1016 s-1.
For n is real and the waves propagate freely. For n is pure imaginary and the field is exponentially attenuated with the distance from the surface. Therefore the radiation is reflected from the surface. Therefore, for visible and infrared radiation < P and n is imaginary. In general, n is complex because of :
NONLINEAR SUSCEPTIBILITY Dipole moment per unit volume or polarization in the linear case The general form of polarization in a nonlinear medium is
E x JUSTIFICATION OF THE PRESENCE OF A NONLINEAR RESPONSE If the force exercised by the electric field of the wave becomes comparable with the Coulomb’s force between the electron and the nucleus, the oscillator is perturbed (anharmonic oscillator) and, at the lower level of the perturbation, we can write:
The solution of eq.(4) can be expressed as the sum of two terms in which x(1)(t) is obtained solving eq.(4) without the anharmonic term, whereas x(2)(t) is considered a small correction of the solution at the first order x(1)(t) and is obtained utilizing x(1)(t) in the anharmonic term In this way, considering the case in which the forcing electric field is formed by the sum of two fields at different frequencies
We have the solution at the first order and subsequently the solution at the second order, solving eq.(6) with the use of (8) is in which
Therefore the solution of the second order brings to the generation of oscillations at a frequency different from the ones of the forcing field. In particular, it is possible to have frequencies equal to the sum or to the difference of the field frequencies or to the double (second harmonic). Moreover, we emphasize that the previous formulas remain valid also if just a single forcing field is present. In this case x(2)(t) will be the sum of a second harmonic term (2) and a null pulsation term (term of optical rectification).
Remembering the expression for the medium polarization, we can write where N is the number of dipoles for volume unit which, compared with (10) permits to write
SECOND HARMONIC PRODUCTION The nonlinear properties in the optical region have been demonstrated for the first time in 1961 by Franken et al. during an experiment of second harmonic generation. Sending red light of a ruby laser ( = 6.943 Å) onto a crystal of quartz, they observed ultraviolet light.
The story is that when Franken published his paper on the second harmonic production, the proof reader corrected the photo, suppressing the tiny spot of the second harmonic believing it was just a smash. You may see this on the photo below in which under the arrow you see….nothing!
In many crystals the nonlinear polarization depends on the direction of propagation, on the polarization of the electric field and on the orientation of the optical axis of the crystal. Since in such materials the vectors P and E are not necessarily parallel, the coefficient is a tensor. The second order polarization can be written as where i, j, k represent the coordinates x, y, z. The main part of the coefficients dijk, however, are usually zero and so only a few of them must be considered.
Only the non-centrosymmetric crystals can have a non null tensor dijk. In facts, let us consider an isotropic crystal. In this case dijk is independent from the direction and therefore it is constant. If now we invert the direction of the electric field, also the polarization must change sign, that is It is clear that, not being able to be , dijk must be null. Moreover, in materials for which d ≠ 0, since no physical meaning can be assigned to an exchange of Ej with Ek, it must be dijk = dikj.
Now if we consider the Maxwell equations writing we have The polarization can be written as the sum of a linear term plus a nonlinear one In case of materials with second order nonlinearity PNL may be written as
So eq.(16) can be written, assuming j = 0 from which If we consider the unidimensional case of propagation along a direction z, we have
Let us consider now three monochromatic fields with frequencies 1, 2, 3 using the complex notation where the indices i, j, k represent the components x or y. The polarization at frequency 1 = 3 - 2, for example, from (18) and from (22) results
Substituting eqs.(22) into (21) for the component E1i, it is necessary to calculate If we assume we have with similar expressions for
Finally, substituting (26) and (23) into (21) we have and in analogous way The second harmonic field is obtained immediately from (27) and (28) for the case of 1 = 2 and 3 = 21. Therefore it is enough to consider only, f.e., (27) and the last one of (28).
To further simplify the analysis we can assume that the power lost by the frequency 1 (fundamental) is negligible, and therefore So it is sufficient to consider just the last one of (28) where and
In eq.(31) is the constant of propagation of the beam at 1 polarized in the direction i. The solution of (30) for E3j(0) = 0 for a crystal of length L is or According to (32) a requirement for an efficient second harmonic generation is that k = 0, that is from (31) with 3 = 2, 1 = 2 =
If k ≠ 0, the second harmonic wave generated at a generic plane z1 which propagates until another plane z2 is not in phase with that generated in z2. This produces an interference described by the factor in (32). The condition is never practically satisfied because, due to dispersion, the refractive index depends on .
In general we have being and therefore
Coherence length We have no more second harmonic production when sin(ΔkL/2)/ΔkL/2 = 0 This is achieved when ΔkL/2 =π Which means L = 2π/Δk L is named coherence lenght.
However, it is possible to make k = 0 (phase-matching condition) using various skills; the most used of which takes advantage from the natural birefringence of the anisotropic crystals. From (34) we can see that k = 0 implies so that the refractive indices of second harmonic and of fundamental frequency have to be equal. Using birefringent materials it is possible to fulfill the condition of phase matching.
As another example a PBG may be used to obtain phase matching
Finally we point out that very well known electro-optic effects discovered in the XIX century are particular cases of nonlinear optics. Pockels effectΔεr = qEo P = εoχEεr = 1 + χ P = εoχE + χ(2) Eo E = εo(χ + χ(2) /εo Eo )E = εoχ’E χ’ = χ+ χ(2) /εo Eo 1+ εr + Δεr = 1 + εr +χ(2) /εo Eo Δεr = χ(2) / εo Eo
Kerr effect Δεr = qEo2 P = εoχEεr = 1 + χ P = εoχE + χ(3) Eo2 E = εo(χ + χ(3) /εo Eo2 )E = εoχ’E χ’ = χ+ χ(3) /εo Eo2 1+ εr + Δεr = 1 + εr +χ(3) /εo Eo2 Δεr = χ(3) / εo Eo2
Nonlinear Optical Interactions • The E-field of a laser beam • 2nd order nonlinear polarization
2nd Order Nonlinearities • The incident optical field • Nonlinear polarization contains the following terms
Sum Frequency Generation Application: Tunable radiation in the UV Spectral region.